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Find out when the Aggregates Levy does not apply to the intended products of an exempt process.
An accelerated licensing process may apply to some applications for dredging activity.
Proficiency testing (PT), also known as external quality assessment (EQA), allows the introduction of samples of known but undisclosed content into a laboratory’s routine testing procedure.
Follow this guidance when you want to get spend approval for digital and technology activities.
An evaluation focusing on the delivery of the scheme, what has worked well and less well in its implementation, and any lessons to be learned.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Organisational definitions of terms concerned with risk and risk-related matters.
Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
The Ministry of Defence's approach to procurement, and where to find defence opportunities.
To be completed by overseas authorities when making a request for Service of Process to the UK. Date: Fri Sep 21 11:09:30 BST 2012…
How to serve legal documents overseas and take evidence abroad.
This study reflects on 3 visualizations created during a 3 year long collaboration.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
These principles describe how the government should manage legacy technology.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Guidance on tests and inspections for producers, processors, importers and sellers of organic food, feed and seed.
When you export goods outside the UK for processing or repair and then re-import them, you can use outward processing to reduce your duty payments.
Reduce development overhead and time to deployment by standardising how teams design, launch and manage APIs in your organisation.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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